Canonical Allele Identifier: CA1257754916
Gene: MEIS1 HGNC NCBI

Linked Data

dbSNP Id: rs1572900155

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.66554346A>G , CM000664.2:g.66554346A>G GRCh38
NC_000002.11:g.66781478A>G , CM000664.1:g.66781478A>G GRCh37
NC_000002.10:g.66634982A>G NCBI36
NG_011467.1:g.123947A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272369.14:c.965+6327A>G MANE Select ENSP00000272369.8:n.965+6327A>G
ENST00000272369.13:c.965+6327A>G ENSP00000272369.8:n.965+6327A>G
ENST00000398506.6:c.959+6327A>G ENSP00000381518.2:n.959+6327A>G
ENST00000409517.5:n.279+6327A>G
ENST00000450027.2:n.420+6327A>G
ENST00000475239.5:n.525+6327A>G
ENST00000488550.5:c.965+6327A>G ENSP00000475161.1:n.965+6327A>G
ENST00000495021.6:c.770+6327A>G ENSP00000440571.1:n.770+6327A>G
ENST00000542964.5:n.398+6327A>G
ENST00000560281.6:c.965+6327A>G ENSP00000454209.1:n.965+6327A>G
ENST00000606455.5:n.419+6327A>G
NM_002398.2:c.965+6327A>G NP_002389.1:n.965+6327A>G
XM_005264321.1:c.1013+6327A>G XP_005264378.1:n.1013+6327A>G
XM_005264322.1:c.965+6327A>G XP_005264379.1:n.965+6327A>G
XM_005264323.1:c.1013+6327A>G XP_005264380.1:n.1013+6327A>G
XM_005264324.3:c.770+6327A>G XP_005264381.1:n.770+6327A>G
XM_005264325.3:c.770+6327A>G XP_005264382.1:n.770+6327A>G
XR_244932.1:n.1599+6327A>G
XR_244933.1:n.1599+6327A>G
NM_002398.3:c.965+6327A>G MANE Select NP_002389.1:n.965+6327A>G